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Analysis of two single nucleotide polymorphisms and loss of heterozygosity detection in the VHL gene in Chinese patients with sporadic renal cell carcinoma

Analysis of two single nucleotide polymorphisms and loss of heterozygosity detection in the VHL gene in Chinese patients with sporadic renal cell carcinoma
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摘要 Renal cell carcinoma (RCC) is the most common malignant tumour in the adult kidney. Recent studies have shown that inactivation of the tumour suppressor gene VHL located in chromosome 3p25-26 region is responsible for sporadic RCCs. According to Kundson's two hit theory, the mechanism of inactivation of a tumour suppressor gene involves mutation, hypermethylation and loss of heterozygosity (LOH). Renal cell carcinoma (RCC) is the most common malignant tumour in the adult kidney. Recent studies have shown that inactivation of the tumour suppressor gene VHL located in chromosome 3p25-26 region is responsible for sporadic RCCs. According to Kundson's two hit theory, the mechanism of inactivation of a tumour suppressor gene involves mutation, hypermethylation and loss of heterozygosity (LOH).
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2005年第15期1291-1294,共4页 中华医学杂志(英文版)
基金 ThisprojectissupportedbytheNationalNaturalScienceFoundationofChina(No.30100184).:Thetwoauthorscontributedequallytothisstudy.
关键词 CARCINOMA renal cell POLYMORPHISM single nucleotide· loss of heterozygosity ·von Hippel-Lindau gene carcinoma, renal cell · polymorphism, single nucleotide· loss of heterozygosity ·von Hippel-Lindau gene
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